Distinguish between spontaneous and induced mutations. Give some examples of mutagens that cause induced mutations.

Short Answer

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Answer: The main difference between spontaneous and induced mutations is that spontaneous mutations occur naturally and randomly during a cell's normal activities, while induced mutations result from exposure to external factors known as mutagens. Examples of mutagens that cause induced mutations include chemical agents (alkylating agents, base analogs, and intercalating agents), physical agents (ultraviolet and ionizing radiation), and biological agents (certain viruses).

Step by step solution

01

Define spontaneous and induced mutations

Spontaneous mutations are changes in the DNA sequence that occur naturally and randomly during a cell's normal activities, such as DNA replication. On the other hand, induced mutations result from exposure to external factors, such as chemicals or radiation, that can alter the DNA sequence.
02

Discuss spontaneous mutations

Spontaneous mutations can occur during DNA replication if DNA polymerase makes a mistake and incorporates an incorrect nucleotide into the sequence. This can lead to base substitutions, insertions, or deletions in the DNA, which may cause changes in an organism's traits. However, spontaneous mutations are relatively rare, because cells have many error-checking mechanisms to fix these mistakes during replication.
03

Discuss induced mutations

Induced mutations are caused by exposure to external factors called mutagens. Mutagens can cause damage to the DNA by altering the structure of the nucleotides, causing crosslinking between the DNA strands, or causing breaks in the DNA backbone. This can lead to a higher mutation rate than spontaneous mutations. Some induced mutations can be harmful, causing diseases like cancer, while others can have no effect or even be beneficial to an organism.
04

Provide examples of mutagens that cause induced mutations

There are various types of mutagens that can cause induced mutations: 1. Chemical mutagens: Examples include alkylating agents (e.g., ethyl methanesulfonate), which add alkyl groups to DNA bases; base analogs (e.g., 5-bromouracil), which resemble natural DNA bases and can be mistakenly incorporated during replication, causing base-pair mismatches; and intercalating agents (e.g., ethidium bromide), which insert themselves between DNA bases, causing insertions or deletions. 2. Physical mutagens: Examples include ultraviolet (UV) radiation, which can cause the formation of pyrimidine dimers in the DNA, leading to errors during replication; and ionizing radiation (e.g., X-rays and gamma rays), which can cause single and double-strand breaks in the DNA. 3. Biological mutagens: Examples include certain viruses, which can insert their own genetic material into the host organism's DNA, causing insertions or deletions, or altering the nucleotide sequence in the process of integration. In summary, spontaneous mutations occur naturally and randomly during a cell's normal activities, whereas induced mutations are the result of exposure to external factors called mutagens. Examples of mutagens that cause induced mutations include chemical agents, radiation, and biological agents.

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Most popular questions from this chapter

In maize, a \(D s\) or \(A c\) transposon can cause mutations in genes at or near the site of transposon insertion. It is possible for these elements to transpose away from their original site, causing a reversion of the mutant phenotype. In some cases, however, even more severe phenotypes appear, due to events at or near the mutant allele. What might be happening to the transposon or the nearby gene to create more severe mutations?

Blectrophilic oxidants are known to create the modified base named 7,8 -dihydro- 8 -axoguanine (oxoG) in DNA. Whereas guanine base-pairs with cytosine, oxoG base-pairs with either cytosine or adenine. (a) What are the sources of reactive oxidants within cells that cause this type of base alteration? (b) Drawing on your knowledge of nucleotide chemistry, draw the structure of \(0 \times 0 \mathrm{G},\) and, below it, draw guanine. Opposite guanine, draw cytosine, including the hydrogen bonds that allow these two molecules to base- pair, Does the structure of oxoG, in contrast to guanine, provide any hint as to why it basepairs with adenine? (c) Assume that an unrepaired oxoG lesion is present in the helix of DNA opposite cytosine. Predict the type of mutation that will occur following several rounds of replication. (d) Which DNA repair mechanisms might work to counteract an oxoG lesion? Which of these is likely to be most effective?

Contrast and compare the mutagenic effects of deaminating agents, alkylating agents, and base analogs.

In this chapter, we focused on how gene mutations arise and how cells repair DNA damage. In particular, we discussed spontaneous and induced mutations, DNA repair methods, and transposable elements, Based on your knowledge of these topics, answer several fundamental questions: (a) How do we know that mutations occur spontaneously? (b) How do we know that certain chemicals and wavelengths of radiation induce mutations in DNA? (c) How do we know that DNA repair mechanisms detect and correct the majority of spontaneous and induced mutations?

In which phases of the cell cycle would you expect double-strand break repair and nonhomologous end joining to occur and why?

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